JP2004502761A - ウイルスポリメラーゼ阻害剤 - Google Patents
ウイルスポリメラーゼ阻害剤 Download PDFInfo
- Publication number
- JP2004502761A JP2004502761A JP2002509292A JP2002509292A JP2004502761A JP 2004502761 A JP2004502761 A JP 2004502761A JP 2002509292 A JP2002509292 A JP 2002509292A JP 2002509292 A JP2002509292 A JP 2002509292A JP 2004502761 A JP2004502761 A JP 2004502761A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cooh
- aryl
- phenyl
- alkenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 0 C*c(cc1OC)ccc1OC Chemical compound C*c(cc1OC)ccc1OC 0.000 description 8
- ZPYJATAERXMSTB-UHFFFAOYSA-N CNC(CN(CCN(CC(O)=O)CC(O)=O)CC(O)=O)=O Chemical compound CNC(CN(CCN(CC(O)=O)CC(O)=O)CC(O)=O)=O ZPYJATAERXMSTB-UHFFFAOYSA-N 0.000 description 5
- WERNCCVZMCGANB-IHWYPQMZSA-N C/C=C(/C(N1)=O)\SC1=S Chemical compound C/C=C(/C(N1)=O)\SC1=S WERNCCVZMCGANB-IHWYPQMZSA-N 0.000 description 3
- ODJCOOCNJCPYTM-UHFFFAOYSA-N CNC(C(C1=O)=O)=C1O Chemical compound CNC(C(C1=O)=O)=C1O ODJCOOCNJCPYTM-UHFFFAOYSA-N 0.000 description 3
- WSIQTSYLPYBXNU-UHFFFAOYSA-N CC(C)(C)OC(NC(Cc(cc1)ccc1OC(C)=O)C(C=[N+]=[N-])=O)=O Chemical compound CC(C)(C)OC(NC(Cc(cc1)ccc1OC(C)=O)C(C=[N+]=[N-])=O)=O WSIQTSYLPYBXNU-UHFFFAOYSA-N 0.000 description 1
- LDCXUSGGLKCAGI-AWEZNQCLSA-N CC(C)(C)OC(N[C@@H](Cc(cc1)ccc1OC(C)=O)C(CBr)=O)=O Chemical compound CC(C)(C)OC(N[C@@H](Cc(cc1)ccc1OC(C)=O)C(CBr)=O)=O LDCXUSGGLKCAGI-AWEZNQCLSA-N 0.000 description 1
- SDJFTIPPLLFDSG-ZDUSSCGKSA-N CC(C)(C)OC(N[C@@H](Cc(cc1)ccc1OC(C)=O)C(O)=O)=O Chemical compound CC(C)(C)OC(N[C@@H](Cc(cc1)ccc1OC(C)=O)C(O)=O)=O SDJFTIPPLLFDSG-ZDUSSCGKSA-N 0.000 description 1
- YSWZAXUSBBYFJX-INIZCTEOSA-N CC(C)(C)OC(N[C@@H](Cc(cc1)ccc1OC(C)=O)c1c[s]c(C)n1)=O Chemical compound CC(C)(C)OC(N[C@@H](Cc(cc1)ccc1OC(C)=O)c1c[s]c(C)n1)=O YSWZAXUSBBYFJX-INIZCTEOSA-N 0.000 description 1
- LPNUHICDAFQUMA-YQCHCMBFSA-N CC(c(cc(C/C(/CCC=O)=N/C(c(cc1)cc2c1[n](C1CCCCC1)c(-c1c[o]cc1)n2)=O)cc1)c1O1)=CC1=O Chemical compound CC(c(cc(C/C(/CCC=O)=N/C(c(cc1)cc2c1[n](C1CCCCC1)c(-c1c[o]cc1)n2)=O)cc1)c1O1)=CC1=O LPNUHICDAFQUMA-YQCHCMBFSA-N 0.000 description 1
- UJHBVMHOBZBWMX-UHFFFAOYSA-N CCOC(c(cc1)cc(N)c1NC1CCCCC1)=O Chemical compound CCOC(c(cc1)cc(N)c1NC1CCCCC1)=O UJHBVMHOBZBWMX-UHFFFAOYSA-N 0.000 description 1
- PALYDABJRIWMKF-UHFFFAOYSA-N CCOC(c(cc1)cc([N+]([O-])=O)c1NC1CCCCC1)=O Chemical compound CCOC(c(cc1)cc([N+]([O-])=O)c1NC1CCCCC1)=O PALYDABJRIWMKF-UHFFFAOYSA-N 0.000 description 1
- FUXQOPCFSOIUQB-UHFFFAOYSA-N CCc(cc1OC)ccc1OCC Chemical compound CCc(cc1OC)ccc1OCC FUXQOPCFSOIUQB-UHFFFAOYSA-N 0.000 description 1
- MWQNNORZVYFWQB-LJQANCHMSA-N C[C@H](c(cc1OC)ccc1OC)NC(c(cc1)cc2c1[n](C1CCCCC1)c(-c1ccccn1)n2)=O Chemical compound C[C@H](c(cc1OC)ccc1OC)NC(c(cc1)cc2c1[n](C1CCCCC1)c(-c1ccccn1)n2)=O MWQNNORZVYFWQB-LJQANCHMSA-N 0.000 description 1
- DQGBRMZAHPCRTH-UHFFFAOYSA-O NC(c1ccc(CC(C(O)=O)NC(c(cc2)cc3c2[n](C2CCCCC2)c(-c2c[o]cc2)n3)=O)cc1)=NN[NH3+] Chemical compound NC(c1ccc(CC(C(O)=O)NC(c(cc2)cc3c2[n](C2CCCCC2)c(-c2c[o]cc2)n3)=O)cc1)=NN[NH3+] DQGBRMZAHPCRTH-UHFFFAOYSA-O 0.000 description 1
- SMSSCMYZICHTDA-UHFFFAOYSA-N OC(COc(cc1)cc2c1cc(CC(C(O)=O)NC(c(cc1)cc3c1[n](C1CCCCC1)c(-c1c[o]cc1)n3)=O)cc2)=O Chemical compound OC(COc(cc1)cc2c1cc(CC(C(O)=O)NC(c(cc1)cc3c1[n](C1CCCCC1)c(-c1c[o]cc1)n3)=O)cc2)=O SMSSCMYZICHTDA-UHFFFAOYSA-N 0.000 description 1
- GDKGIUMLMNQSAL-DEOSSOPVSA-N OC(C[n]1c(ccc(OCC(O)=O)c2)c2c(C[C@@H](C(O)=O)NC(c(cc2)nc3c2[n](C2CCCCC2)c(-c2c[o]cc2)n3)=O)c1)=O Chemical compound OC(C[n]1c(ccc(OCC(O)=O)c2)c2c(C[C@@H](C(O)=O)NC(c(cc2)nc3c2[n](C2CCCCC2)c(-c2c[o]cc2)n3)=O)c1)=O GDKGIUMLMNQSAL-DEOSSOPVSA-N 0.000 description 1
- NQZJRYKGBLFLAJ-MHZLTWQESA-N OCCNC([C@H](Cc(c1c2)c[nH]c1ccc2O)NC(c(cc1)cc2c1[n](C1CCCCC1)c(-c1c[o]cc1)n2)=O)=O Chemical compound OCCNC([C@H](Cc(c1c2)c[nH]c1ccc2O)NC(c(cc1)cc2c1[n](C1CCCCC1)c(-c1c[o]cc1)n2)=O)=O NQZJRYKGBLFLAJ-MHZLTWQESA-N 0.000 description 1
- XXLLGUUTLDYNSS-DEOSSOPVSA-N Oc1ccc(C[C@@H](c2c[s]cn2)NC(c(cc2)cc3c2[n](C2CCCCC2)c(-c2c[o]cc2)n3)=O)cc1 Chemical compound Oc1ccc(C[C@@H](c2c[s]cn2)NC(c(cc2)cc3c2[n](C2CCCCC2)c(-c2c[o]cc2)n3)=O)cc1 XXLLGUUTLDYNSS-DEOSSOPVSA-N 0.000 description 1
- UDUDVSQQEIMVFC-HKBQPEDESA-N Oc1ccc2[nH]cc(C[C@@H](C(NCCN3CCOCC3)=O)NC(c(cc3)cc4c3[n](C3CCCCC3)c(-c3c[o]cc3)n4)=O)c2c1 Chemical compound Oc1ccc2[nH]cc(C[C@@H](C(NCCN3CCOCC3)=O)NC(c(cc3)cc4c3[n](C3CCCCC3)c(-c3c[o]cc3)n4)=O)c2c1 UDUDVSQQEIMVFC-HKBQPEDESA-N 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Virology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21608400P | 2000-07-06 | 2000-07-06 | |
| US27437401P | 2001-03-08 | 2001-03-08 | |
| US28134301P | 2001-04-05 | 2001-04-05 | |
| PCT/CA2001/000989 WO2002004425A2 (en) | 2000-07-06 | 2001-07-04 | Viral polymerase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004502761A true JP2004502761A (ja) | 2004-01-29 |
| JP2004502761A5 JP2004502761A5 (enExample) | 2010-09-09 |
Family
ID=27396228
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002509292A Pending JP2004502761A (ja) | 2000-07-06 | 2001-07-04 | ウイルスポリメラーゼ阻害剤 |
Country Status (11)
| Country | Link |
|---|---|
| US (4) | US6448281B1 (enExample) |
| EP (1) | EP1301487B1 (enExample) |
| JP (1) | JP2004502761A (enExample) |
| AR (1) | AR035038A1 (enExample) |
| AT (1) | ATE346049T1 (enExample) |
| AU (1) | AU2001272258A1 (enExample) |
| CA (1) | CA2412718C (enExample) |
| DE (1) | DE60124718T2 (enExample) |
| ES (1) | ES2276803T3 (enExample) |
| MX (1) | MXPA02012906A (enExample) |
| WO (1) | WO2002004425A2 (enExample) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005501827A (ja) * | 2001-07-20 | 2005-01-20 | ベーリンガー インゲルハイム (カナダ) リミテッド | ウイルスポリメラーゼインヒビター |
| JP2006077004A (ja) * | 2004-08-11 | 2006-03-23 | Chugai Pharmaceut Co Ltd | 抗hcv作用を有する化合物およびそれを含む医薬組成物 |
| WO2007043653A1 (ja) * | 2005-10-13 | 2007-04-19 | Taisho Pharmaceutical Co., Ltd. | ベンゾイミダゾール-5-カルボキサミド誘導体 |
| JP2007537163A (ja) * | 2004-05-06 | 2007-12-20 | サイトキネティクス・インコーポレーテッド | 化合物、組成物、および方法 |
| JP2008506638A (ja) * | 2004-07-16 | 2008-03-06 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ウイルスポリメラーゼインヒビター |
| JP2009525287A (ja) * | 2006-02-03 | 2009-07-09 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ウイルスポリメラーゼインヒビター |
| JP2011503119A (ja) * | 2007-11-16 | 2011-01-27 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ヒト免疫不全ウイルス複製のインヒビター |
| JP2011530531A (ja) * | 2008-08-07 | 2011-12-22 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎ウイルス阻害剤としてのbi−1h−ベンズアミダゾール |
| JP2013532725A (ja) * | 2010-08-04 | 2013-08-19 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎ウイルス阻害剤 |
| JP2018520105A (ja) * | 2015-05-21 | 2018-07-26 | グラクソスミスクライン、インテレクチュアル、プロパテ | Pad4阻害剤としてのベンゾイミダゾール誘導体 |
| JP2018522886A (ja) * | 2015-07-07 | 2018-08-16 | バイエル・ファルマ・アクティエンゲゼルシャフト | mIDH1阻害剤としての2−アリール−および2−アリールアルキル−ベンズイミダゾール |
| JP2020503314A (ja) * | 2016-12-23 | 2020-01-30 | アクイナ ファーマシューティカルズ, インコーポレイテッド | 化合物、組成物、および使用方法 |
Families Citing this family (225)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CZ20013424A3 (cs) * | 1999-12-27 | 2002-02-13 | Japan Tobacco Inc. | Sloučeniny s fúzovanými kruhy a jejich pouľití jako léčiva |
| US6770666B2 (en) | 1999-12-27 | 2004-08-03 | Japan Tobacco Inc. | Fused-ring compounds and use thereof as drugs |
| US6448281B1 (en) * | 2000-07-06 | 2002-09-10 | Boehringer Ingelheim (Canada) Ltd. | Viral polymerase inhibitors |
| US20020165781A1 (en) * | 2000-10-31 | 2002-11-07 | Mckay Brent | Interactive media management system and method for network applications |
| CA2430978C (en) * | 2000-12-28 | 2012-05-15 | Daiichi Pharmaceutical Co., Ltd. | Vla-4 inhibitors |
| EP2048142A3 (en) * | 2001-04-26 | 2009-04-22 | Eisai R&D Management Co., Ltd. | Nitrogen-containing condensed cyclic compound having a pyrazolyl group as a substituent group and pharmaceutical composition thereof |
| US7030150B2 (en) * | 2001-05-11 | 2006-04-18 | Trimeris, Inc. | Benzimidazole compounds and antiviral uses thereof |
| AR035543A1 (es) * | 2001-06-26 | 2004-06-16 | Japan Tobacco Inc | Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con |
| EP2335700A1 (en) * | 2001-07-25 | 2011-06-22 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis C virus polymerase inhibitors with a heterobicylic structure |
| US7294457B2 (en) * | 2001-08-07 | 2007-11-13 | Boehringer Ingelheim (Canada) Ltd. | Direct binding assay for identifying inhibitors of HCV polymerase |
| AU2003248535A1 (en) | 2002-05-20 | 2003-12-12 | Bristol-Myers Squibb Company | Heterocyclicsulfonamide hepatitis c virus inhibitors |
| ES2315568T3 (es) | 2002-05-20 | 2009-04-01 | Bristol-Myers Squibb Company | Inhibidores del virus de la hepatitis c basados en cicloalquilo p1' sustituido. |
| PL215228B1 (pl) | 2002-05-20 | 2013-11-29 | Bristol Myers Squibb Co | Zwiazki tripeptydowe, ich zastosowanie i kompozycja farmaceutyczna je zawierajaca oraz jej zastosowanie |
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| TW200400818A (en) | 2002-05-21 | 2004-01-16 | Wyeth Corp | Method for the use of pyranoindole derivatives to treat infection with hepatitis C virus |
| TW200400963A (en) | 2002-05-21 | 2004-01-16 | Wyeth Corp | R-enantiomers of pyranoindole derivatives and the use thereof for the treatment of hepatitis C virus infection or disease |
| WO2003101993A1 (en) * | 2002-06-04 | 2003-12-11 | Neogenesis Pharmaceuticals, Inc. | Pyrazolo` 1,5a! pyrimidine compounds as antiviral agents |
| US7041690B2 (en) | 2002-07-01 | 2006-05-09 | Pharmacia & Upjohn Company, Llc | Inhibitors of HCV NS5B polymerase |
| BR0305259A (pt) | 2002-07-01 | 2004-10-05 | Upjohn Co | Inibidores de hcv ns5b polimerase |
| GB0215293D0 (en) | 2002-07-03 | 2002-08-14 | Rega Foundation | Viral inhibitors |
| US6812363B2 (en) * | 2002-10-15 | 2004-11-02 | Usv Limited | Racemization of optically active 2-substituted phenyl glycine esters |
| WO2004041795A1 (en) * | 2002-10-30 | 2004-05-21 | Guilford Pharmaceuticals Inc. | Novel inhibitors of dipeptidyl peptidase iv |
| US7902203B2 (en) | 2002-11-01 | 2011-03-08 | Abbott Laboratories, Inc. | Anti-infective agents |
| US7151114B2 (en) | 2003-01-09 | 2006-12-19 | Boehringer Ingelheim International Gmbh | Use of substituted 2-phenylbenzimidazoles as medicaments |
| US7098231B2 (en) * | 2003-01-22 | 2006-08-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| US7223785B2 (en) * | 2003-01-22 | 2007-05-29 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| GB0307891D0 (en) * | 2003-04-04 | 2003-05-14 | Angeletti P Ist Richerche Bio | Chemical compounds,compositions and uses |
| ATE422895T1 (de) | 2003-04-16 | 2009-03-15 | Bristol Myers Squibb Co | Makrocyclische isochinolinpeptidinhibitoren des hepatitis-c-virus |
| WO2004099241A1 (en) * | 2003-05-09 | 2004-11-18 | Boehringer Ingelheim International Gmbh | Hepatitis c virus ns5b polymerase inhibitor binding pocket |
| SE0301446D0 (sv) * | 2003-05-16 | 2003-05-16 | Astrazeneca Ab | New Compounds |
| US7304085B2 (en) * | 2003-06-04 | 2007-12-04 | Genelabs Technologies, Inc. | Nitrogen-containing heteroaryl derivatives |
| JP4676884B2 (ja) | 2003-07-24 | 2011-04-27 | 第一三共株式会社 | シクロヘキサンカルボン酸類 |
| BRPI0413234A (pt) * | 2003-08-01 | 2006-10-03 | Genelabs Tech Inc | derivados de imidazola bicìclica contra flaviviridae |
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| JP2011503119A (ja) * | 2007-11-16 | 2011-01-27 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ヒト免疫不全ウイルス複製のインヒビター |
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Also Published As
| Publication number | Publication date |
|---|---|
| US20030232816A1 (en) | 2003-12-18 |
| MXPA02012906A (es) | 2004-07-30 |
| DE60124718T2 (de) | 2007-09-13 |
| WO2002004425A3 (en) | 2002-04-25 |
| AR035038A1 (es) | 2004-04-14 |
| US20040224955A1 (en) | 2004-11-11 |
| DE60124718D1 (de) | 2007-01-04 |
| US6448281B1 (en) | 2002-09-10 |
| CA2412718C (en) | 2010-06-22 |
| US20020065418A1 (en) | 2002-05-30 |
| US7439258B2 (en) | 2008-10-21 |
| WO2002004425A2 (en) | 2002-01-17 |
| EP1301487A2 (en) | 2003-04-16 |
| AU2001272258A1 (en) | 2002-01-21 |
| US6794404B2 (en) | 2004-09-21 |
| EP1301487B1 (en) | 2006-11-22 |
| ATE346049T1 (de) | 2006-12-15 |
| ES2276803T3 (es) | 2007-07-01 |
| US6479508B1 (en) | 2002-11-12 |
| CA2412718A1 (en) | 2002-01-17 |
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